Fucoxanthin-Rich Brown Algae Extract Improves Male Reproductive Function on Streptozotocin-Nicotinamide-Induced Diabetic Rat Model.
Zwe-Ling KongSabri SudirmanYu-Chun HsuChieh-Yu SuHsiang-Ping KuoPublished in: International journal of molecular sciences (2019)
Hypogonadism and oxidative stress are occurring commonly in men with diabetes and associated male infertility. This study aimed to investigate the capability of anti-oxidative and anti-inflammatory properties of fucoxanthin as well as to evaluate its protective effects on male reproduction in diabetic rats. The RAW 264.7 macrophage cells were used to evaluate the anti-oxidative and anti-inflammatory activity. Thirty male Sprague-Dawley rats were induced by streptozotocin-nicotinamide for a diabetes model and fed either with three different doses of fucoxanthin (13, 26, and 65 mg/kg) or rosiglitazone (0.571 mg/kg) for four weeks. The fucoxanthin significantly inhibited nitric oxide production and reduced reactive oxygen species level in lipopolysaccharide-induced RAW 264.7 cells. In the animal study, fucoxanthin administration improved insulin resistance, restored sperm motility, decreased abnormal sperm number, and inhibited lipid peroxidation. Moreover, it restored GPR54 and SOCS-3 mRNA expression in the hypothalamus and recovered luteinizing hormone level, as well as the testosterone level. In conclusion, fucoxanthin not only possessed antioxidant and anti-inflammatory properties but also decreased the diabetes signs and symptoms as well as improved spermatogenesis and male reproductive function.
Keyphrases
- diabetic rats
- oxidative stress
- induced apoptosis
- anti inflammatory
- type diabetes
- lipopolysaccharide induced
- insulin resistance
- nitric oxide
- cardiovascular disease
- glycemic control
- ischemia reperfusion injury
- reactive oxygen species
- dna damage
- cell cycle arrest
- inflammatory response
- adipose tissue
- high fat diet
- signaling pathway
- depressive symptoms
- skeletal muscle
- metabolic syndrome
- replacement therapy
- endothelial cells
- staphylococcus aureus
- escherichia coli
- polycystic ovary syndrome
- biofilm formation
- cell proliferation
- nitric oxide synthase
- physical activity
- stress induced